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Methyl 2-bromo-3-(4-fluorophenyl)propanoate → Methyl 3-(4-fluorophenyl)propanoate

HRID 647430
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HRID 647430 반응식
Br[CH:2]([CH2:7][C:8]1[CH:13]=[CH:12][C:11]([F:14])=[CH:10][CH:9]=1)[C:3]([O:5][CH3:6])=[O:4]>C(O)(=O)C.[Zn]>[F:14][C:11]1[CH:10]=[CH:9][C:8]([CH2:7][CH2:2][C:3]([O:5][CH3:6])=[O:4])=[CH:13][CH:12]=1
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참가 물질

4

반응물 1

HCID 12188683Methyl 2-bromo-3-(4-fluorophenyl)propanoate

생성물 1

HCID 22906572Methyl 3-(4-fluorophenyl)propanoate

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

Crude methyl 2-bromo-3-(4-fluorophenyl)propionate in acetic acid (330 ml) was stirred and treated with zinc dust (32.75 g) in portions over 30 minutes. The mixture was stirred for an additional 30 minutes and filtered, and the filter cake was washed with acetic acid. After the filtrate was evaporated the residue was partitioned between methylene chloride and water to give crude methyl 3-(4-fluorophenyl)propionate, which was refluxed with aqueous sodium hydroxide (400 ml, 10%) for 2 hrs, cooled, treated with decolorizing carbon, and filtered. The filtrate was acidified with 5 N HCl and filtered. The filter cake was washed extensively with water to give 3-(4-fluorophenyl)propionic acid (20.0 g) as colourless crystals, mp 90° C.

후처리

  1. filtrationfiltered
  2. washthe filter cake was washed with acetic acid
  3. customAfter the filtrate was evaporated the residue
  4. customwas partitioned between methylene chloride and water

출처 및 근거

ORD 기록
ord-d68543213f61443bad84c49c21c173eb
출처 데이터셋
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04409017

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